Medical Devices
NMPA issues Guidelines for Technical Review of the Registration of Synthetic Resin Teeth and Others
Updated: Jul 6, 2019
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To strengthen the supervision and guidance over the registration of medical device products and further improve the quality of registration review, NMPA organized the formulation of and published the Guidelines for Technical Review of the Registration of Synthetic Resin Teeth, the Guidelines for Technical Review of the Registration of IUD, and the Guidelines for Technical Review of the Registration of Implantable Drug Delivery System on May 22, 2019.
